Team:Glendale CC AZ/Protocols/Ligation
From 2013.igem.org
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== Procedure == | == Procedure == | ||
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+ | 1. Add 2µL of digested plasmid backbone | ||
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+ | 2. Add equimolar amount of digested Part 1 | ||
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+ | 3. Add equimolar amount of digested Part 2 | ||
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+ | 4. Add 1µL T4 DNA ligase buffer. | ||
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+ | 5. Add 0.5µL T4 DNA ligase. | ||
+ | |||
+ | 6. Add water to 10µL. | ||
+ | |||
+ | 7. Place in pre-programmed thermal cycler at 16°C for 30 minutes then at 80°C for 20 minutes. |
Revision as of 22:57, 26 August 2013
Ligation Protocol
Protocol from: http://parts.igem.org/Help:Protocols/Ligation
Materials
-digested plasmid backbone -equimolar amount of EcoRI-HF SpeI digested fragment -equimolar amount of XbaI PstI digested fragment -T4 DNA ligase buffer -T4 DNA ligase -dH2O
Procedure
1. Add 2µL of digested plasmid backbone
2. Add equimolar amount of digested Part 1
3. Add equimolar amount of digested Part 2
4. Add 1µL T4 DNA ligase buffer.
5. Add 0.5µL T4 DNA ligase.
6. Add water to 10µL.
7. Place in pre-programmed thermal cycler at 16°C for 30 minutes then at 80°C for 20 minutes.